82613-27-2

Upstream product

• 1679-18-1 4-Chlorophenylboronic acid 
• 1356399-96-6 (Z)-1-(4-chlorophenyl)-2-(phenylsulfonyl)ethenamine 
• 39511-12-1 (E)-3-(furan-2-yl)-1-phenyl-2-propen-1-one 
• 14385-65-0 (2E)-1-(4-chlorophenyl)-3-(2-furyl)prop-2-en-1-one 
• 16883-69-5 N-phenacylpyridinium bromide 

Relevant academic research and scientific papers

Synthesis of unsymmetrical polysubstituted pyridines from β-sulfonylvinylamines via 1-aza-allyl anion intermediates

A modular synthesis of highly functionalized unsymmetrical pyridines has been developed from reacting β-sulfonylvinylamines with α,β-unsaturated systems in the presence of base via the formation of 1-aza-allyl anion intermediates. Georg Thieme Verlag Stut

Synthesis of Some New 2,4,6-Triarylpyridines Using Phenacylpyridinium Ylid

Phenacylpyridinium ylid reacts with some substituted benzylidene-2-acetothiophenes, benzylidene-4-chloroacetophenones and benzylidene-3-nitroacetophenones in the presence of ammonium acetate in methanol or glacial acetic acid to give 2-phenyl-4-substituted-phenyl-6-(2-thienyl)pyridines (5a-e), 2-phenyl-4-substituted-phenyl-6-(4-chlorophenyl)pyridines (5f-j) and 2-phenyl-4-substituted-phenyl-6-(3-nitrophenyl)pyridines (5k-m), respectively in fair to good yields.